RNA表观遗传学在癌症:当前的知识和治疗意义

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2025-08-03 DOI:10.1002/mco2.70322
Shanhe Huang, Zonglin Li, Weilong Lin, Ruihui Xie, Hai Huang
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引用次数: 0

摘要

RNA表观遗传学,也被称为表观转录组学,已经成为癌症生物学中一个关键的调控层,超出了传统DNA和组蛋白修饰的范围。它包括一系列动态的转录后过程,包括RNA生物合成、剪接、运输、稳定性、降解、翻译和化学修饰,这些过程由RNA结合蛋白(rbp)和非编码RNA (ncRNAs)精心策划。总的来说,这些机制影响mRNA的命运,塑造转录输出,并重新编程肿瘤微环境。重要的是,编码RNA和ncRNA本身都受到表观遗传调控,形成复杂的反馈回路,促进肿瘤发生、免疫逃避、转移和治疗耐药性。在这篇综述中,我们系统地综合了目前对肿瘤进展过程中RNA代谢和RNA表观遗传修饰的理解,特别关注rbp和RNA修饰的作用。此外,我们重点介绍了基于rna的治疗策略的最新进展,包括mRNA疫苗、反义寡核苷酸、sirna和环状rna支架。这些创新的方法为靶向转录活跃但在基因组上“不可药物”的癌症驱动因素提供了有希望的途径。总之,我们的合成为理解肿瘤生物学中的RNA表观遗传学提供了一个全面的框架,并为转录组可塑性指导的精确肿瘤学奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

RNA Epigenetics in Cancer: Current Knowledge and Therapeutic Implications

RNA Epigenetics in Cancer: Current Knowledge and Therapeutic Implications

RNA epigenetics, also referred to as epitranscriptomics, has emerged as a critical regulatory layer in cancer biology, extending beyond the scope of traditional DNA and histone modifications. It encompasses a series of dynamic posttranscriptional processes—including RNA biosynthesis, splicing, transport, stability, degradation, translation, and chemical modifications—orchestrated by RNA-binding proteins (RBPs) and noncoding RNAs (ncRNAs). Collectively, these mechanisms influence mRNA fate, shape transcriptional output, and reprogram the tumor microenvironment. Importantly, both coding RNA and ncRNA are themselves subjected to epigenetic regulation, forming intricate feedback loops that contribute to oncogenesis, immune evasion, metastasis, and therapeutic resistance. In this review, we systematically synthesize the current understanding of RNA metabolism and RNA epigenetic modifications during tumor progression, with a particular focus on the roles of RBPs and RNA modifications. Furthermore, we highlight recent advances in RNA-based therapeutic strategies, including mRNA vaccines, antisense oligonucleotides, siRNAs, and circRNA scaffolds. These innovative approaches offer promising avenues for targeting transcriptionally active yet genomically “undruggable” cancer drivers. Together, our synthesis provides a comprehensive framework for understanding RNA epigenetics in tumor biology and lays the groundwork for precision oncology guided by transcriptome plasticity.

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来源期刊
CiteScore
6.70
自引率
0.00%
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审稿时长
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